Vanadium(IV) oxide

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Vanadium(IV) oxide
Vanadium(IV) oxide
IUPAC name
Vanadium(IV) oxide
Other names
Vanadium dioxide
Vanadium tetroxide
12036-21-4 YesY
PubChem 82849
Molar mass 82.94 g/mol
Appearance Deep Blue Powder
Density 4.571 g/cm3 (monoclinic)
4.653 g/cm3 (tetragonal)
Melting point 1,967 °C
Distorted rutile (<70 °C, monoclinic)
Rutile (>70 °C, tetragonal)
R-phrases 36/37/38
S-phrases 26-36/37/39
NFPA 704
Flammability code 0: Will not burn. E.g., water Health code 2: Intense or continued but not chronic exposure could cause temporary incapacitation or possible residual injury. E.g., chloroform Reactivity code 0: Normally stable, even under fire exposure conditions, and is not reactive with water. E.g., liquid nitrogen Special hazards (white): no codeNFPA 704 four-colored diamond
Flash point Non-flammable
Related compounds
Other anions
Vanadium disulfide
Vanadium diselenide
Vanadium ditelluride
Other cations
Niobium(IV) oxide
Tantalum(IV) oxide
Vanadium(II) oxide
Vanadium(III) oxide
Vanadium(V) oxide
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Infobox references

Vanadium(IV) dioxide is an inorganic compound with the formula VO2. It is a dark blue solid. Vanadium(IV) dioxide is amphoteric, dissolving in non-oxidising acids to give the blue vanadyl ion, [VO]2+ and in alkali to give the brown [V4O9]2− ion, or at high pH [VO4]4−.[1] VO2 has a phase transition very close to room temperature(~66 °C). Electrical resistivity, opacity, etc, can change up several orders. Due to these properties, it has been widely used in surface coating,[2] sensors,[3] and imaging.[4] Potential applications include use in memory devices.[5]



At temperatures below Tc=340 K, VO
has a monoclinic (space group P21/c) crystal structure. Above Tc, the structure is tetragonal, like rutile TiO
. In the monoclinic phase, the V4+ ions form pairs along the c axis, leading to alternate short and long V-V distances of 2.65 Å and 3.12 Å. In comparison, in the rutile phase the V4+ ions are separated by a fixed distance of 2.96 Å. As a result, the number of V4+ ions in the crystallographic unit cell doubles from the rutile to the monoclinic phase.[6]

The equilibrium morphology of rutile VO
particles is acicular, laterally confined by (110) surfaces, which are the most stable termination planes.[7] The surface tends to be oxidized with respect to the stoichiometric composition, with the oxygen adsorbed on the (110) surface forming vanadyl species.[7] The presence of V5+ ions at the surface of VO
films has been observed by x-ray photoelectron spectroscopy (XPS) measurements.[8]


At the rutile to monoclinic transition temperature, VO
also exhibits a metal to semiconductor transition in its electronic structure: the rutile phase is metallic while the monoclinic phase is semiconducting.[9] The optical band gap of VO2 in the low-temperature monoclinic phase is about 0.7 eV.[10]

Synthesis and structure[edit]

Following the method described by Berzelius, VO
is prepared by comproportionation of vanadium(III) oxide and vanadium(V) oxide:[11]

+ V
→ 4 VO

At room temperature VO2 has a distorted rutile structure with shorter distances between pairs of V atoms indicating metal-metal bonding. Above 68 °C the structure changes to an undistorted rutile structure and the metal-metal bonds are broken causing an increase in electrical conductivity and magnetic susceptibility as the bonding electrons are "released".[1][12] The origin of this insulator to metal transition remains controversial and is of interest in condensed matter physics.

Infrared reflectance[edit]

expresses temperature-dependent reflective properties. When heated from room temperature to 80 °C, the material's thermal radiation rises normally until 74 °C, before suddenly appearing to drop around 20 °C. At room temperature VO
is almost transparent to infrared light. As its temperature rises it gradually changes to reflective. At intermediate temperatures it behaves as a highly absorbing dielectric.[13][14]

A thin film of vanadium oxide on a highly reflecting substrate (for specific infrared wavelengths) such as sapphire is either absorbing or reflecting, dependent on temperature. Its emissivity varies considerably with temperature. When the vanadium oxide transitions with increased temperature, the structure undergoes a sudden decrease in emissivity – looking colder to infrared cameras than it really is.[13]

Varying the substrate materials e.g., to indium tin oxide, and modifying the vanadium oxide coating using doping, straining and other processes, alter the wavelengths and temperature ranges at which the thermal effects are observed.[13]

Nanoscale structures that appear naturally in the materials' transition region can suppress thermal radiation as the temperature rises. Doping the coating with tungsten lowers the effect's thermal range to room temperature.[13]


Infrared radiation management[edit]

1.9% tungsten-doped material content has been investigated for use as a "spectrally-selective" window coating to block infrared transmission and reduce the loss of building interior heat through windows.[15][16] Varying the amount of tungsten allows regulating the phase transition temperature. The coating has a slight yellow-green color.[17]

Other potential applications of its thermal properties include passive camouflage, thermal beacons, communication or to deliberately speed up or slow down cooling – which could be useful in a variety of structures from homes to satellites.[13]

Nanostars of Vanadium(IV) oxide

Vanadium dioxide can act as extremely fast optical shutters, optical modulators, infrared modulators for missile guidance systems, cameras, data storage, and other applications. The thermochromic phase transition between the transparent semiconductive and reflective conductive phase, occurring at 68 °C, can happen in times as short as 100 femtoseconds.[18]

Phase change computing and memory[edit]

The insulator-metal phase transition in VO2 can be manipulated at the nanoscale using a biased conducting atomic force microscope tip,[19] suggesting applications in computing and information storage.[20]

See also[edit]


  1. ^ a b Greenwood, Norman N.; Earnshaw, Alan (1984). Chemistry of the Elements. Oxford: Pergamon Press. pp. 1144–45. ISBN 0-08-022057-6. 
  2. ^ Li, Yamei; Ji, Shidong; Gao, Yanfeng; Luo, Hongjie; Kanehira, Minoru (2013-04-02). "Core-shell VO2@TiO2 nanorods that combine thermochromic and photocatalytic properties for application as energy-saving smart coatings". Scientific Reports. 3. doi:10.1038/srep01370. PMC 3613806free to read. PMID 23546301. 
  3. ^ Hu, Bin; Ding, Yong; Chen, Wen; Kulkarni, Dhaval; Shen, Yue; Tsukruk, Vladimir V.; Wang, Zhong Lin (2010-12-01). "External-Strain Induced Insulating Phase Transition in VO2 Nanobeam and Its Application as Flexible Strain Sensor". Advanced Materials. 22 (45): 5134–5139. doi:10.1002/adma.201002868. ISSN 1521-4095. 
  4. ^ Gurvitch, M.; Luryi, S.; Polyakov, A.; Shabalov, A. (2009-11-15). "Nonhysteretic behavior inside the hysteresis loop of VO2 and its possible application in infrared imaging". Journal of Applied Physics. 106 (10): 104504. doi:10.1063/1.3243286. ISSN 0021-8979. 
  5. ^ Xie, Rongguo; Bui, Cong Tinh; Varghese, Binni; Zhang, Qingxin; Sow, Chorng Haur; Li, Baowen; Thong, John T. L. (2011-05-10). "An Electrically Tuned Solid-State Thermal Memory Based on Metal–Insulator Transition of Single-Crystalline VO2 Nanobeams". Advanced Functional Materials. 21 (9): 1602–1607. doi:10.1002/adfm.201002436. ISSN 1616-3028. 
  6. ^ Morin, F. J. (1959). "Oxides Which Show a Metal-to-Insulator Transition at the Neel Temperature". Physical Review Letters. 3 (1): 34–36. doi:10.1103/PhysRevLett.3.34. ISSN 0031-9007. 
  7. ^ a b Mellan, Thomas A.; Grau-Crespo, Ricardo (2012). "Density functional theory study of rutile VO2 surfaces". The Journal of Chemical Physics. 137 (15): 154706. doi:10.1063/1.4758319. ISSN 0021-9606. 
  8. ^ Manning, Troy D.; Parkin, Ivan P.; Pemble, Martyn E.; Sheel, David; Vernardou, Dimitra (2004). "Intelligent Window Coatings: Atmospheric Pressure Chemical Vapor Deposition of Tungsten-Doped Vanadium Dioxide". Chemistry of Materials. 16 (4): 744–749. doi:10.1021/cm034905y. ISSN 0897-4756. 
  9. ^ Goodenough, John B. (1971-11-01). "The two components of the crystallographic transition in VO2". Journal of Solid State Chemistry. 3 (4): 490–500. doi:10.1016/0022-4596(71)90091-0. 
  10. ^ Shin, S.; Suga, S.; Taniguchi, M.; Fujisawa, M.; Kanzaki, H.; Fujimori, A.; Daimon, H.; Ueda, Y.; Kosuge, K. "Vacuum-ultraviolet reflectance and photoemission study of the metal-insulator phase transitions in VO 2 , V 6 O 13 , and V 2 O 3". Physical Review B. 41 (8): 4993–5009. doi:10.1103/physrevb.41.4993. 
  11. ^ Handbook of Preparative Inorganic Chemistry, 2nd Ed. Edited by G. Brauer, Academic Press, 1963, NY. Vol. 1. p. 1267.
  12. ^
  13. ^ a b c d e "Natural metamaterial looks cooler when heated". Retrieved 2014-01-01. 
  14. ^ Kats, M. A.; Blanchard, R.; Zhang, S.; Genevet, P.; Ko, C.; Ramanathan, S.; Capasso, F. (2013). "Vanadium Dioxide as a Natural Disordered Metamaterial: Perfect Thermal Emission and Large Broadband Negative Differential Thermal Emittance". Physical Review X. 3 (4). doi:10.1103/PhysRevX.3.041004. 
  15. ^ "Sol-Gel Vanadium oxide". Retrieved 2012-09-12. 
  16. ^ "Intelligent Window Coatings that Allow Light In but Keep Heat Out - News Item". Retrieved 2012-09-12. 
  17. ^ "Eye on Technology". oe magazine. 2009-11-03. Retrieved 2012-09-12. 
  18. ^ "Timing nature's fastest optical shutter". Retrieved 2012-09-12. 
  19. ^ Jeehoon Kim; Ko, Changhyun; Frenzel, Alex; Ramanathan, Shriram; Hoffman, Jennifer E. (2010). "Nanoscale imaging and control of resistance switching in VO2 at room temperature". Applied Physics Letters. 96: 213106. doi:10.1063/1.3435466. 
  20. ^ Zhou, You; Ramanathan, S. (2015-08-01). "Mott Memory and Neuromorphic Devices". Proceedings of the IEEE. 103 (8): 1289–1310. doi:10.1109/JPROC.2015.2431914. ISSN 0018-9219.